Ludman Sian, Jafari-Mamaghani Mehrdad, Ebling Rosemary, Fox Adam T, Lack Gideon, Du Toit George
Royal London Hospital, Barts Health NHS Trust, London, UK.
Immunodiagnostics Division, Thermo Fisher Scientific, Uppsala, Sweden.
Pediatr Allergy Immunol. 2016 Mar;27(2):134-40. doi: 10.1111/pai.12504. Epub 2015 Dec 9.
There is limited information regarding the onset and sensitization patterns of pollen food syndrome (PFS) in children. The aim was to explore this within children referred to a specialist allergy clinic at a London Tertiary Hospital.
A total of 54 patients with seasonal allergic rhinitis (SAR) were enrolled in equal numbers in three age groups; 0-5, 6-10, 11-15 years. Families completed a questionnaire on rhinitis, food symptoms and quality of life. Children underwent skin prick testing (SPT) to fresh fruits, nuts and a blood test for microarray analysis.
Clinical diagnosis of PFS was made in 26/54 (48%), increasing with age (group 1 = 3 (17%), group 2 = 9 (50%), group 3 = 14 (78%) (p = 0.03)). Microarray demonstrates children aged 2.8 years sensitized to pan-allergens and 4.5 years symptomatic to pan-allergens. Peach, cherry, carrot and strawberry SPT had the highest sensitivity and NPV at 100%. The sensitivity of PR10 molecules on microarray was 92%, PPV 62% and NPV 87%. Microarray confirmed 69% of allergens on clinical history compared to 61% by SPT. Microarray and SPT had a 19% false-negative rate. The quality-of-life data showed moderate impact across all domains, and patients with PFS were significantly more likely to have increased anxiety over time spent preparing food (p = 0.029).
We demonstrate that SAR occurs in children from 1.4 years and PFS from 4.5 years with a changing pattern of pan-allergen sensitization. Microarray and SPT have moderate concordance in confirming allergens. PFS impacts negatively on quality of life and should be assessed in all paediatric allergy patients.
关于儿童花粉食物综合征(PFS)的发病及致敏模式的信息有限。本研究旨在对伦敦一家三级医院专科过敏门诊的儿童进行相关情况的探索。
共纳入54例季节性过敏性鼻炎(SAR)患者,平均分为三个年龄组:0 - 5岁、6 - 10岁、11 - 15岁。家属完成一份关于鼻炎、食物症状及生活质量的问卷。儿童接受针对新鲜水果、坚果的皮肤点刺试验(SPT)及用于微阵列分析的血液检测。
54例患者中26例(48%)被临床诊断为PFS,且随年龄增长而增加(第1组 = 3例(17%),第2组 = 9例(50%),第3组 = 14例(78%)(p = 0.03))。微阵列分析显示,2.8岁儿童对泛过敏原致敏,4.5岁儿童出现泛过敏原症状。桃、樱桃、胡萝卜和草莓的SPT敏感性和阴性预测值最高,均为100%。微阵列上PR10分子的敏感性为92%,阳性预测值为62%,阴性预测值为87%。与SPT相比,微阵列根据临床病史确认了69%的过敏原,而SPT为61%。微阵列和SPT的假阴性率为19%。生活质量数据显示在所有领域均有中度影响,且PFS患者随着准备食物时间的增加,焦虑情绪明显更易加重(p = 0.029)。
我们证明,SAR在1.4岁儿童中出现以及PFS在4.5岁儿童中出现,且泛过敏原致敏模式不断变化。微阵列和SPT在确认过敏原方面有中度一致性。PFS对生活质量有负面影响,应在所有儿科过敏患者中进行评估。